Canonical Allele Identifier: CA408630280
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33408801C>G , CM000682.2:g.33408801C>G GRCh38
NC_000020.10:g.31996607C>G , CM000682.1:g.31996607C>G GRCh37
NC_000020.9:g.31460268C>G NCBI36
NG_011622.1:g.40092G>C , LRG_332:g.40092G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.1325G>C MANE Select ENSP00000217381.2:p.Arg442Pro
ENST00000217381.2:c.1325G>C ENSP00000217381.2:p.Arg442Pro
NM_003098.2:c.1325G>C , LRG_332t1:c.1325G>C NP_003089.1:p.Arg442Pro
XM_005260517.1:c.1325G>C XP_005260574.1:p.Arg442Pro
XM_011529007.1:c.1357G>C XP_011527309.1:p.Glu453Gln
XM_011529008.1:c.1357G>C XP_011527310.1:p.Glu453Gln
XR_936612.1:n.1361G>C
XM_024451971.1:c.998G>C XP_024307739.1:p.Arg333Pro
NM_003098.3:c.1325G>C MANE Select NP_003089.1:p.Arg442Pro